FDA Inspection 1027723 — DMS Holdings, Inc.

DMS Holdings, Inc. — FEI 1000143485

The FDA completed an inspection of DMS Holdings, Inc. on September 18, 2017 in Waukegan, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 18, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Waukegan, IL (United States)